International safety notice
This product is used when intubating a tracheal tube. We have recently discovered that products that do not meet the specified suction volume may be being shipped, so we have voluntarily implemented a voluntary recall of the affected products. I decided to collect it.
Japan / PMDA Recalls · JPN · Nov 28, 2023
Key facts
| Title | This product is used when intubating a tracheal tube. We have recently discovered that products that do not meet the specified suction volume may be being shipped, so we have voluntarily implemented a voluntary recall of the affected products. I decided to collect it. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Flexible laryngoscope Brand name: Laryngeal fiberscope OLYMPUS LF-GP |
| Manufacturer | Olympus Medical Systems Co., Ltd. |
| Models | 2616083, 2817374 |
| Date | Nov 28, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1